GKN1-miR-185-DNMT1 axis suppresses gastric carcinogenesis through regulation of epigenetic alteration and cell cycle

Jung Hwan Yoon, Yoo Jin Choi, Won Suk Choi, Hassan Ashktorab, Duane T. Smoot, Suk Woo Nam, Jung Young Lee, Won Sang Park

Research output: Contribution to journalArticle

Abstract

Purpose: Gastrokine 1 (GKN1) functions to protect the gastric antral mucosa and promotes healing by facilitating restoration and proliferation after injury. GKN1 is downregulated in Helicobacter pylori-infected gastric epithelial cells and loss of GKN1 expression is closely associated with gastric carcinogenesis, but underlying mechanisms of the tumor-suppressing effects of GKN1 remain largely unknown. Experimental Design: AGS, MKN1, MKN28 gastric cancer cells and HFE-145 immortalized nonneoplastic gastric mucosal cells were transfected with GKN1 or shGKN1. We conducted molecular and functional studies of GKN1 and miR-185 and investigated the mechanisms of alteration. We also analyzed epigenetic alterations in 80 gastric cancer tissues. Results: Restoration of GKN1 protein suppressed gastric cancer cell growth by inducing endogenous miR-185 that directly targets epigenetic effectors DNMT1 and EZH2 in gastric cancer cells. In addition, ectopic expression of GKN1 upregulated Tip60 and downregulated HDAC1 in an miR-185-independent manner, thereby inducing cell-cycle arrest by regulating cell-cycle proteins in gastric cancer cells. Notably, GKN1expression was inversely correlated withDNMT1and EZH2 expression in a subset of 80 gastric cancer tissues and various gastric cancer cell lines. Interestingly, it was found that GKN1 exerted a synergistic anti-cancerous effect with 5-fluorouracil on tumor cell growth, which suggests a possible therapeutic intervention method for gastric cancer. Conclusion: Our results show that GKN1 has an miR-185-dependent and -independent mechanism for chromatic and DNA epigenetic modification, thereby regulating the cell cycle. Thus, the loss of GKN1 function contributes to malignant transformation and proliferation of gastric epithelial cells in gastric carcinogenesis.

Original languageEnglish (US)
Pages (from-to)4599-4610
Number of pages12
JournalClinical Cancer Research
Volume19
Issue number17
DOIs
StatePublished - Sep 1 2013
Externally publishedYes

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Epigenomics
Stomach Neoplasms
Stomach
Cell Cycle
Carcinogenesis
Down-Regulation
Epithelial Cells
Cell Cycle Proteins
Growth
Gastric Mucosa
Cell Cycle Checkpoints
Helicobacter pylori
Fluorouracil
Neoplasms
Research Design
Color
Cell Line
DNA
Wounds and Injuries
Proteins

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Yoon, J. H., Choi, Y. J., Choi, W. S., Ashktorab, H., Smoot, D. T., Nam, S. W., ... Park, W. S. (2013). GKN1-miR-185-DNMT1 axis suppresses gastric carcinogenesis through regulation of epigenetic alteration and cell cycle. Clinical Cancer Research, 19(17), 4599-4610. https://doi.org/10.1158/1078-0432.CCR-12-3675

GKN1-miR-185-DNMT1 axis suppresses gastric carcinogenesis through regulation of epigenetic alteration and cell cycle. / Yoon, Jung Hwan; Choi, Yoo Jin; Choi, Won Suk; Ashktorab, Hassan; Smoot, Duane T.; Nam, Suk Woo; Lee, Jung Young; Park, Won Sang.

In: Clinical Cancer Research, Vol. 19, No. 17, 01.09.2013, p. 4599-4610.

Research output: Contribution to journalArticle

Yoon, JH, Choi, YJ, Choi, WS, Ashktorab, H, Smoot, DT, Nam, SW, Lee, JY & Park, WS 2013, 'GKN1-miR-185-DNMT1 axis suppresses gastric carcinogenesis through regulation of epigenetic alteration and cell cycle', Clinical Cancer Research, vol. 19, no. 17, pp. 4599-4610. https://doi.org/10.1158/1078-0432.CCR-12-3675
Yoon, Jung Hwan ; Choi, Yoo Jin ; Choi, Won Suk ; Ashktorab, Hassan ; Smoot, Duane T. ; Nam, Suk Woo ; Lee, Jung Young ; Park, Won Sang. / GKN1-miR-185-DNMT1 axis suppresses gastric carcinogenesis through regulation of epigenetic alteration and cell cycle. In: Clinical Cancer Research. 2013 ; Vol. 19, No. 17. pp. 4599-4610.
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AU - Lee, Jung Young

AU - Park, Won Sang

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